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Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells

Curcumin exerts beneficial effects on cardiovascular diseases, including hypertension. However, its mechanisms are unknown. We propose that curcumin prevents the development of hypertension by regulating AT(1) receptor (AT(1)R) expression in arteries. The present study examined how curcumin regulate...

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Autores principales: Yao, Yonggang, Wang, Wei, Li, Meixiang, Ren, Hongmei, Chen, Caiyu, Wang, Jialiang, Wang, Wei Eric, Yang, Jian, Zeng, Chunyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857140/
https://www.ncbi.nlm.nih.gov/pubmed/27146402
http://dx.doi.org/10.1038/srep25579
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author Yao, Yonggang
Wang, Wei
Li, Meixiang
Ren, Hongmei
Chen, Caiyu
Wang, Jialiang
Wang, Wei Eric
Yang, Jian
Zeng, Chunyu
author_facet Yao, Yonggang
Wang, Wei
Li, Meixiang
Ren, Hongmei
Chen, Caiyu
Wang, Jialiang
Wang, Wei Eric
Yang, Jian
Zeng, Chunyu
author_sort Yao, Yonggang
collection PubMed
description Curcumin exerts beneficial effects on cardiovascular diseases, including hypertension. However, its mechanisms are unknown. We propose that curcumin prevents the development of hypertension by regulating AT(1) receptor (AT(1)R) expression in arteries. The present study examined how curcumin regulates AT(1)R expression in vascular smooth muscle cells and investigated the physiological significance of this regulation in angiotensin (Ang) II-induced hypertension. The results showed that curcumin decreased AT(1)R expression in a concentration- and time-dependent manner in vascular smooth muscle cells. Using luciferase reporters with an entire AT(1) or a mutant AT(1)R in A10 cells, the AT(1)R promoter activity was inhibited by 10(−6 )M curcumin, and the proximal element (from −61 to +25 bp) of the AT(1)R promoter was crucial for curcumin-induced AT(1)R down-regulation. An electrophoretic mobility shift assay showed that curcumin decreased specificity protein 1 (SP1) binding with the AT(1)R promoter in A10 cells. Curcumin treatment reduced Ang II-induced hypertension in C57Bl/6J mice, which was accompanied by lower AT(1)R expression in the arteries and decreased Ang II-mediated vasoconstriction in the mesenteric artery. These findings indicate that curcumin down-regulates AT(1)R expression in A10 cells by affecting SP1/AT(1)R DNA binding, thus reducing AT(1)R-mediated vasoconstriction and subsequently prevents the development of hypertension in an Ang II-induced hypertensive model.
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spelling pubmed-48571402016-05-19 Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells Yao, Yonggang Wang, Wei Li, Meixiang Ren, Hongmei Chen, Caiyu Wang, Jialiang Wang, Wei Eric Yang, Jian Zeng, Chunyu Sci Rep Article Curcumin exerts beneficial effects on cardiovascular diseases, including hypertension. However, its mechanisms are unknown. We propose that curcumin prevents the development of hypertension by regulating AT(1) receptor (AT(1)R) expression in arteries. The present study examined how curcumin regulates AT(1)R expression in vascular smooth muscle cells and investigated the physiological significance of this regulation in angiotensin (Ang) II-induced hypertension. The results showed that curcumin decreased AT(1)R expression in a concentration- and time-dependent manner in vascular smooth muscle cells. Using luciferase reporters with an entire AT(1) or a mutant AT(1)R in A10 cells, the AT(1)R promoter activity was inhibited by 10(−6 )M curcumin, and the proximal element (from −61 to +25 bp) of the AT(1)R promoter was crucial for curcumin-induced AT(1)R down-regulation. An electrophoretic mobility shift assay showed that curcumin decreased specificity protein 1 (SP1) binding with the AT(1)R promoter in A10 cells. Curcumin treatment reduced Ang II-induced hypertension in C57Bl/6J mice, which was accompanied by lower AT(1)R expression in the arteries and decreased Ang II-mediated vasoconstriction in the mesenteric artery. These findings indicate that curcumin down-regulates AT(1)R expression in A10 cells by affecting SP1/AT(1)R DNA binding, thus reducing AT(1)R-mediated vasoconstriction and subsequently prevents the development of hypertension in an Ang II-induced hypertensive model. Nature Publishing Group 2016-05-05 /pmc/articles/PMC4857140/ /pubmed/27146402 http://dx.doi.org/10.1038/srep25579 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yao, Yonggang
Wang, Wei
Li, Meixiang
Ren, Hongmei
Chen, Caiyu
Wang, Jialiang
Wang, Wei Eric
Yang, Jian
Zeng, Chunyu
Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells
title Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells
title_full Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells
title_fullStr Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells
title_full_unstemmed Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells
title_short Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT(1) Receptor in Vascular Smooth Muscle Cells
title_sort curcumin exerts its anti-hypertensive effect by down-regulating the at(1) receptor in vascular smooth muscle cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857140/
https://www.ncbi.nlm.nih.gov/pubmed/27146402
http://dx.doi.org/10.1038/srep25579
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